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Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis
PURPOSE: In the study of microbial keratitis, in vivo animal models often require a large number of animals, and in vitro monolayer cell culture does not maintain the three-dimensional structure of the tissues or cell-to-cell communication of in vivo models. Here, we propose reproducible ex vivo mod...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285415/ https://www.ncbi.nlm.nih.gov/pubmed/27844206 http://dx.doi.org/10.1007/s00417-016-3546-0 |
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author | Pinnock, Abigail Shivshetty, Nagaveni Roy, Sanhita Rimmer, Stephen Douglas, Ian MacNeil, Sheila Garg, Prashant |
author_facet | Pinnock, Abigail Shivshetty, Nagaveni Roy, Sanhita Rimmer, Stephen Douglas, Ian MacNeil, Sheila Garg, Prashant |
author_sort | Pinnock, Abigail |
collection | PubMed |
description | PURPOSE: In the study of microbial keratitis, in vivo animal models often require a large number of animals, and in vitro monolayer cell culture does not maintain the three-dimensional structure of the tissues or cell-to-cell communication of in vivo models. Here, we propose reproducible ex vivo models of single- and dual-infection keratitis as an alternative to in vivo and in vitro models. METHODS: Excised rabbit and human corneoscleral rims maintained in organ culture were infected using 10(8) cells of Staphylococcus aureus, Pseudomonas aeruginosa, Candida albicans or Fusarium solani. The infection was introduced by wounding with a scalpel and exposing corneas to the microbial suspension or by intrastromal injection. Post-inoculation, corneas were maintained for 24 and 48 h at 37 °C. After incubation, corneas were either homogenised to determine colony-forming units (CFU)/cornea or processed for histological examination using routine staining methods. Single- and mixed-species infections were compared. RESULTS: We observed a significant increase in CFU after 48 h compared to 24 h with S. aureus and P. aeruginosa. However, no such increase was observed in corneas infected with C. albicans or F. solani. The injection method yielded an approximately two- to 100-fold increase (p < 0.05) in the majority of organisms from infected corneas. Histology of the scalpel-wounded and injection models indicated extensive infiltration of P. aeruginosa throughout the entire cornea, with less infiltration observed for S. aureus, C. albicans and F. solani. The models also supported dual infections. CONCLUSIONS: Both scalpel wounding and injection methods are suitable for inducing infection of ex vivo rabbit and human cornea models. These simple and reproducible models will be useful as an alternative to in vitro and in vivo models for investigating the detection and treatment of microbial keratitis, particularly when this might be due to two infective organisms. |
format | Online Article Text |
id | pubmed-5285415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-52854152017-02-13 Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis Pinnock, Abigail Shivshetty, Nagaveni Roy, Sanhita Rimmer, Stephen Douglas, Ian MacNeil, Sheila Garg, Prashant Graefes Arch Clin Exp Ophthalmol Basic Science PURPOSE: In the study of microbial keratitis, in vivo animal models often require a large number of animals, and in vitro monolayer cell culture does not maintain the three-dimensional structure of the tissues or cell-to-cell communication of in vivo models. Here, we propose reproducible ex vivo models of single- and dual-infection keratitis as an alternative to in vivo and in vitro models. METHODS: Excised rabbit and human corneoscleral rims maintained in organ culture were infected using 10(8) cells of Staphylococcus aureus, Pseudomonas aeruginosa, Candida albicans or Fusarium solani. The infection was introduced by wounding with a scalpel and exposing corneas to the microbial suspension or by intrastromal injection. Post-inoculation, corneas were maintained for 24 and 48 h at 37 °C. After incubation, corneas were either homogenised to determine colony-forming units (CFU)/cornea or processed for histological examination using routine staining methods. Single- and mixed-species infections were compared. RESULTS: We observed a significant increase in CFU after 48 h compared to 24 h with S. aureus and P. aeruginosa. However, no such increase was observed in corneas infected with C. albicans or F. solani. The injection method yielded an approximately two- to 100-fold increase (p < 0.05) in the majority of organisms from infected corneas. Histology of the scalpel-wounded and injection models indicated extensive infiltration of P. aeruginosa throughout the entire cornea, with less infiltration observed for S. aureus, C. albicans and F. solani. The models also supported dual infections. CONCLUSIONS: Both scalpel wounding and injection methods are suitable for inducing infection of ex vivo rabbit and human cornea models. These simple and reproducible models will be useful as an alternative to in vitro and in vivo models for investigating the detection and treatment of microbial keratitis, particularly when this might be due to two infective organisms. Springer Berlin Heidelberg 2016-11-14 2017 /pmc/articles/PMC5285415/ /pubmed/27844206 http://dx.doi.org/10.1007/s00417-016-3546-0 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Basic Science Pinnock, Abigail Shivshetty, Nagaveni Roy, Sanhita Rimmer, Stephen Douglas, Ian MacNeil, Sheila Garg, Prashant Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title | Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title_full | Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title_fullStr | Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title_full_unstemmed | Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title_short | Ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
title_sort | ex vivo rabbit and human corneas as models for bacterial and fungal keratitis |
topic | Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5285415/ https://www.ncbi.nlm.nih.gov/pubmed/27844206 http://dx.doi.org/10.1007/s00417-016-3546-0 |
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